OCULAR MYOPATHY WITH CURARE SENSITIVITY
General Information (adopted from Orphanet):
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Synonyms, Signs:
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Number of Symptoms
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12
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OrphanetNr:
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OMIM Id:
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257600
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ICD-10:
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UMLs:
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MeSH:
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MedDRA:
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Snomed:
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Prevalence, inheritance and age of onset:
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Prevalence:
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No data available.
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Inheritance:
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Autosomal recessive inheritance
[Omim]
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Age of onset:
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Juvenile onset
Childhood onset
[Omim]
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Disease classification (adopted from Orphanet):
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Parent Diseases:
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No data available.
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1
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(HPO:0008507)
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Static ophthalmoparesis |
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1 / 7739
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2
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(HPO:0001939)
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Abnormality of metabolism/homeostasis |
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328 / 7739
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3
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(HPO:0003198)
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Myopathy |
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151 / 7739
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4
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(HPO:0003690)
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Limb muscle weakness |
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41 / 7739
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5
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(HPO:0000007)
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Autosomal recessive inheritance |
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2538 / 7739
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6
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(HPO:0003621)
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Juvenile onset |
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105 / 7739
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7
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(HPO:0011463)
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Childhood onset |
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65 / 7739
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8
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(OMIM)
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No oropharyngeal weakness |
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1 / 7739
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9
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(OMIM)
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Normal tetanic stimulation of ulnar nerve |
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1 / 7739
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10
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(OMIM)
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Curare sensitivity |
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1 / 7739
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11
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(OMIM)
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No response to neostigmine or edrophonium |
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1 / 7739
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12
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(OMIM)
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Ocular myopathy |
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1 / 7739
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |